(Q32143975)

English

congenital stationary night blindness autosomal dominant 1

A congenital stationary night blindness characterized by autosomal dominant inheritance that has material basis in mutations in the RHO gene on chromosome 3q22.1.

  • rhodopsin-related congenital stationary night blindness
  • CSNBAD1
  • NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1
  • congenital stationary night blindness autosomal dominant type 1
  • Night Blindness, Congenital Stationary, Autosomal Dominant type 1
  • Night Blindness, Congenital Stationary, Rhodopsin-Related
  • NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1

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